Vericert

Specialized Expertise in Medical Device Compliance

• With decades of combined experience, our team understands the complex global regulatory frameworks—including CDSCO (India), USFDA (USA), CE (Europe), Health Canada, and more. We offer precise guidance for your Class I, II, III, and IV medical devices, ensuring smooth registration, documentation, and licensing.

Certified ISO Consultants

• We are IRCA-certified Lead Auditors and ISO implementation experts, offering consultancy and audit support across ISO 13485 (Medical Devices), ISO 9001 (Quality Management), ISO 22716 (Cosmetics GMP), ISO 14001 (Environment), ISO 45001 (Occupational Health & Safety), and more.

End-to-End Support

• From documentation to audit preparation, training, implementation, and post-certification maintenance—we deliver complete consultancy packages under one roof. Whether you're a startup or an established manufacturer, our team tailors services to your exact needs.

100+ Regulatory Success Stories

• We've successfully guided over 100 clients through licensing with CDSCO, USFDA, and Health Canada. Our proven track record includes device master file preparation, technical files, risk management, PMS, CER, and sterilization validation.

Timely & Transparent Process

• We value your time. Our consultants provide realistic timelines, fixed deliverables, and proactive communication to ensure a smooth and stress-free compliance journey.

Global Experience, Local Insight

• We serve clients across India, the Middle East, Europe, and North America. With deep knowledge of both local and international requirements, we help you bridge the gap to global markets.